Search results for " impr"

showing 10 items of 877 documents

Introduction to MIP synthesis, characteristics and analytical application

2019

Abstract One of the trends in analytical chemistry is associated with designing and developing new types of sample preparation techniques, which might significantly increase the efficiency and selectivity of the analytes isolation or/and preconcentration process. One of the most widely employed solutions is selective sorption materials, defined as molecularly imprinted polymers (MIPs), as well as the sorbents with the molecular fingerprint. Due to their simple preparation protocol, mechanical, thermal and chemical stability and selectivity, MIPs have found application as a stationary phase in separation techniques such as liquid chromatography or capillary electrophoresis, in electrochemica…

chemistry.chemical_classificationAnalyteMaterials scienceChromatographyCapillary electrophoresischemistryExtraction (chemistry)Molecularly imprinted polymerSorptionSample preparationChemical stabilityPolymer
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Water-compatible molecularly imprinted polymers obtained via high-throughput synthesis and experimental design.

2003

A technique allowing high-throughput synthesis and evaluation of molecularly imprinted polymer sorbents at a reduced scale (mini-MIPs) was developed and used for the optimization of MIPs for use in pure aqueous environments. The technique incorporated a 4-port liquid-handling robot for the rapid dispensing of monomers, templates, solvents and initiator into the reaction vessels of a 96-well plate. A library of 80 polymers, each ca. 50 mg, could thus be prepared in 24 h. The MIP rebinding capacity and selectivity could be rapidly assessed in the batch mode by quantifying nonbound fractions in parallel using a UV monochromator plate reader. This allowed a complete evaluation of the binding ch…

chemistry.chemical_classificationAqueous solutionMolecularly imprinted polymerNanotechnologyGeneral ChemistryPolymerBiochemistryCatalysischemistry.chemical_compoundColloid and Surface ChemistryTemplateMonomerMolecular recognitionchemistryChemical engineeringMolecular imprintingSelectivityJournal of the American Chemical Society
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Application of Molecular Imprinted Polymers for Selective Solid Phase Extraction of Bisphenol A

2016

Abstract Selective molecularly imprinted polymers (MIPs) with bisphenol A as template were synthesized using the non-covalent imprinting approach. MIPs were prepared using thermally initiated polymerization with 1,1’-azobis(cyclohexanecarbonitryle) (ACHN) as initiator and ethylene glycol dimethacrylate (EDMA) as a cross-linking agent. The tested functional monomers included methacrylic acid, acrylamide, and 4-vinylpyridine. The selectivity of the BPA-MIP for the solid phase extraction of bisphenol A was tested in samples containing other related alkylphenols. The polymers prepared in acetonitrile using methacrylic acid or acrylamide as monomer showed the highest selectivity towards target a…

chemistry.chemical_classificationBisphenol AEnvironmental Engineering010401 analytical chemistryMolecularly imprinted polymerPolymer010501 environmental sciences01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryEnvironmental ChemistryOrganic chemistrySolid phase extraction0105 earth and related environmental sciencesEcological Chemistry and Engineering S
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Surface initiated molecularly imprinted polymer films: a new approach in chiral capillary electrochromatography

2001

A new generation of imprinted composite particles was tested as capillary electrochromatography stationary phase. Silica particles characterised by a well defined particle size (10 µm diameter), shape and pore system (1000 A) were modified with an azoinitiator and subsequently used to graft molecularly imprinted polymers targeted to bind L-phenylalanine anilide. Fused silica capillaries were packed over a length corresponding to 8 cm, using a pneumatic amplification pump, and the stationary phase thus obtained was tested with respect to its electrochromatographic performance. The electroendosmotic flow mobility was evaluated with respect to both the different content of polymer on the silic…

chemistry.chemical_classificationCapillary electrochromatographyAnalytical chemistryMolecularly imprinted polymerPolymerBiochemistryAnalytical ChemistryCapillary electrophoresischemistryElectrochromatographyPhase (matter)ElectrochemistryEnvironmental ChemistryParticle sizeSelectivitySpectroscopyThe Analyst
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Noncovalent molecular imprinting: antibody-like molecular recognition in polymeric network materials

1997

Abstract Molecular imprinting techniques allow the preparation of polymeric receptors which bind small molecules with affinities and selectivities of the same order as those observed in the binding of antigens by antibodies. The molecular imprinting technology has now reached a stage where the commercial use of imprinted materials is being assessed, notably for separations requiring strong and selective binding of small molecules. This development is driven by the potential advantages of polymeric receptors over biological in terms of stability, capacity, cost and ease of preparation. In this short review the state of the art of noncovalent imprinting is summarised indicating a few areas in…

chemistry.chemical_classificationChemistryPolymerCombinatorial chemistryAffinitiesSmall moleculeAnalytical ChemistryMolecular recognitionPolymer chemistryMoleculeSurface modificationImprinting (psychology)Molecular imprintingSpectroscopyTrAC Trends in Analytical Chemistry
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Influence of the pH on the behavior of an imprinted polymeric stationary phase--supporting evidence for a binding site model.

2001

The equilibrium isotherms of the two enantiomers of phenylalanine anilide (PA) were measured by conventional frontal analysis at three different pH on a thermally-treated imprinted stationary phase selective for the L enantiomer. The first of these pH (buffer pH=3.0, pH(app)=4.0) is well below the apparent pKa (6.4) of the two solutes, the second (buffer pH=5.8, pH(app)=7.0) slightly below this pKa, and the third (buffer pH=7.0, pH(app)=8.3) well above it. The experimental data were fitted to several isotherm models. The best estimates of the parameters of these models are reported and discussed. The corresponding isotherms are compared with the experimental ones. The contributions of the e…

chemistry.chemical_classificationChromatographyChemistryHydrogen bondPolymersCarboxylic acidPhenylalanineOrganic ChemistryBinding energyAnalytical chemistryPhenylalanineStereoisomerismStereoisomerismGeneral MedicineHydrogen-Ion ConcentrationBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryEnantiomerMolecular imprintingJournal of chromatography. A
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Application of Imprinted Synthetic Polymers in Binding Assay Development

2000

The first part of the review describes a method for the synthesis of molecularly imprinted polymers for use in binding assays. The method considers the many factors involved that affect the recognition properties of the materials and describes an approach to screening and optimization of these factors. The second part describes the development of binding assays using such polymers. This includes the use of different labels, the effect of solvent and buffer, the scale of the assay (amount of solid polymer), and how these influence the quality of the assay in terms of sensitivity, selectivity, and speed of analysis.

chemistry.chemical_classificationChromatographyChromatographyPolymersLigand binding assayDrug Evaluation PreclinicalMolecular ConformationMolecularly imprinted polymerPolymerBuffersLigandsSensitivity and SpecificityGeneral Biochemistry Genetics and Molecular BiologyPharmaceutical PreparationschemistrySolventsAdsorptionSelectivityMolecular BiologyMethods
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Application of molecularly imprinted polymers in supercritical fluid chromatography

2000

Molecularly imprinted polymers (MIPs), for the templates free base racemic propranolol and the L-enantiomer of phenylalanine anilide (L-PA), were investigated as stationary phases in supercritical fluid chromatography (SFC). Large retention differences were observed on the propranolol MIP for both the template molecule and the structural analogue metoprolol compared to that observed on the corresponding blank polymer. Mobile phase composition and solute concentration were found to affect this retention behaviour. The phenylalanine anilide MIP (L-PA MIP) was found to be enantioselective in SFC with stronger retention observed for the template enantiomer. Throughout the study, characteristic …

chemistry.chemical_classificationChromatographyChromatographyPolymersOrganic ChemistryMolecularly imprinted polymerFree baseGeneral MedicinePolymerPropranololBiochemistryHigh-performance liquid chromatographySupercritical fluidAnalytical ChemistrychemistrySupercritical fluid chromatographyEnantiomerMolecular imprintingChromatography High Pressure LiquidJournal of Chromatography A
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Imprinted chiral stationary phases in high-performance liquid chromatography

2001

Polymers imprinted with chiral templates offer a new generation of tailor-made chiral stationary phases (CSPs) with predictable selectivities. This review summarizes the present state of the art of molecular imprinting to generate tailor-made CSPs and provides an overview of the main factors involved in the manufacturing process that are crucial to the chromatographic performance of the phases.

chemistry.chemical_classificationChromatographyManufacturing processChemistryOrganic ChemistryStereoisomerismGeneral MedicinePolymerBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryTemplatePhase compositionEnantiomerMolecular imprintingChirality (chemistry)Chromatography High Pressure LiquidJournal of Chromatography A
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Development of a semiautomated procedure for the synthesis and evaluation of molecularly imprinted polymers applied to the search for functional mono…

2001

Abstract A previously described scaled-down version of the established monolith procedure, where molecularly imprinted polymers (MIPs) are prepared on the bottom surface of chromatographic vials [Anal. Chem. 71 (1999) 2092] has been here further optimised with respect to its full automation. The protocol results in savings of time and reagents compared to the monolith procedure, allowing ca. 60 polymers (∼50 mg each) to be synthesised in parallel. Both blank and imprinted polymers are then evaluated in situ by equilibrium batch rebinding tests. Each step in the synthesis and evaluation was considered with the aim of achieving an automated method with wide applicability with regards to templ…

chemistry.chemical_classificationChromatographyMolecularly imprinted polymerPolymerBiochemistryDissociation (chemistry)Analytical Chemistrychemistry.chemical_compoundMonomerTemplatechemistryPolymerizationEnvironmental ChemistryMoleculeSelectivitySpectroscopyAnalytica Chimica Acta
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